Beer Process
Beer Process
Beer Process
and
Critical Control Points
(HACCP)
Plan for the
Canadian Brewing Industry
A Project of
Brewers Association of Canada
HACCP Working Group
Revision Date: November 2009
www.brewers.ca
Table of Contents
Introduction.............................................................................................................5
HACCP (Hazard Analysis Critical Control Point) systems are required under
proposed Health Canadas Good Manufacturing Practices Regulations for Food.
Specifically, manufacturers must develop procedures to ensure products
manufactured do not pose a health risk.
This manual deals in detail with steps 1 through 8, which include Principles 1
through 3 of HACCP system elements. It also discusses in general terms the
follow-up requirements that make up steps 9 through 12.
It is suggested that the user of this document becomes acquainted with the BAC
Food Safety Toolkit Introduction document before attempting to proceed with
applying the recommendations herein.
There are also other BAC guidance documents that are to be used along with
this BAC - Generic HACCP Plan model. They are:
Reminder - This document is not a customized model per se. Each brewery using
this working guide is responsible for producing its own customized HACCP
program.
The BAC HACCP Working Group was established under the direction of the
Product Integrity Committee of the Brewers Association of Canada.
On the basis of available information for each of the ingredients used in beer and
for each of the process steps in brewing, potential biological, physical and
chemical hazards are identified. Information sources include published
databases, scientific literature, company records, external and internal audits etc.
In addition to identifying potential hazards, Forms 5, 6 and 7 are used to identify
the control points.
Critical Control Points for breweries are determined using the HACCP Decision
Tree. The Decision Tree was first developed by a Codex Alimentarius working
group on HACCP in June 1991. This Decision Tree has been slightly modified to
include a prescreening question and preliminary instructions.
Using the Decision Tree, Form 8 is completed. The last column is where Critical
Control Points are identified. CCPs are labelled numerically with a category
qualifier for Biological, Physical and Chemical (B, P or C) hazard and expected
outcome of the control measure (elimination of risk(e), prevention (p), or
minimize or reduce (r)). In this model , the Critical Control Points in breweries were identified
as follows:
Step CCP #
Empty Bottle Inspection CCP1-P
Empty Bottle Inspection/ Residual Liquid Detector CCP1-C
Filling (Auto-Flush Only) CCP2-P
Internal Cleaning (Manual) CCP3-C
Hazards identified on Forms 5, 6 and 7 are either controlled at some point in the
brewing process or cannot be controlled by the facility. Form 9 is intended to
identify control measures that do not take place in the brewery but are controlled
elsewhere. No such hazards were identified in the analysis of breweries.
For each Critical Control Point, critical limits were established. These are values
which separate acceptability from unacceptability. They are intended to meet
government regulations, industry standards or other scientific data.
At each CCP, the monitoring requirements and the means to ensure that the CCP
remains within the critical limits are specified. Monitoring procedures generally
relate to on-line processes and are usually by observation or by measurement.
The frequency of testing, who is responsible for carrying out the testing, and the
testing procedures must also be specified. The monitoring specifications are
written on Form 10 for each CCP. Each brewery will develop its own
specifications, where required.
Monitoring tracks the system's operation and allows for action to be taken in the
event of a loss of control or where there is a trend toward the loss of control. It
provides information to a brewery on a timely basis, allowing for decisions on the
acceptability of the lot at a particular stage in the process. Monitoring procedures
There are many ways to monitor critical control points. Monitoring can be done
on a continuous or batch basis. The reliability of continuous monitoring (100 % is
preferred where feasible). The established monitoring frequency must be
sufficient to substantiate that the hazard is under control. Responsibility for
monitoring is clearly identified and individuals monitoring the CCPs must be
trained in the testing procedure and must fully understand the purpose and
importance of monitoring. The individual must have ready access to the
monitoring activity and must be unbiased in monitoring and reporting. Finally the
individual must accurately report the monitoring activity.
All operational records and documents that are associated with CCP monitoring
must be properly completed and signed by the person doing the monitoring and
verified/signed by a responsible official of the company.
Validation ensures that the plans do what they were designed to do;
that is, they are successful in ensuring the production of safe
product. Plants will be required to validate their own HACCP plans.
Verification activities are methods, procedures and tests used to determine if the
HACCP plans for that establishment are valid and are operating properly.
Verification activities are generally involved and may include analytical testing. In
carrying out the verification activities, the establishment may find that some
hazards were overlooked or they may discover new or unexpected hazards. In
this case, the plan needs to be modified appropriately. The verification
procedures at each CCP are written on Form 10 by each brewery in accordance
with the brewery requirements. Both the establishment and the CFIA will have a
role in verifying HACCP plan compliance and will carry out activities to verify that
the HACCP plan is operating properly. Verification activities differ from monitoring
activities. Results from verification activities are not intended to make decisions
on the acceptability of lots of product. Verification activities involve for example,
analytical testing or auditing of the monitoring procedures, product sampling,
audits of monitoring and verification records.
The HACCP records are defined as the record keeping that is done at each CCP
and that contain the information required to ensure that the HACCP plan is
followed.
Monitoring results are documented together with any deviations and corrective
action taken. Failure to document the control of a CCP would be a critical
departure from the HACCP plan. Verification activities are also to be recorded.
Records must specify who recorded the information and must indicate who
reviewed and signed off the information.
PRODUCT/PROCESS
DESCRIPTION
2. Important Product 3
Characteristics
(aw, pH, PRESERVATIVES..)
3. How it is to be used Consumer product - Alcoholic beverage
6. Where it will be sold Government sales provisions apply - licensed retailers, hotels
etc.
On premise and off premise
7. Labelling Instructions Food and Drug Regulations (i.e. alcohol content labelling)
Consumer Packaging and Labelling Legislative/Regulatory
requirements
Claims allowed by Health Canada (i.e. energy value)
8. Special Distribution Inspection done on third party carriers and carriers dedicated to
Control food
LIST OF PRODUCT
INGREDIENTS AND
INCOMING MATERIALS
Title: Form 2 -
BAC Generic List of Product Ingredients and Incoming Materials
Completed By: BAC TC Date:
Approved By: BAC TC Date:
Page 1 of 12
KEY
P
Physical Hazard identified at this step
MASTER FLOWCHART OF
MAJOR PROCESS STEPS (PS) FOR MAKING BEER (Page 2 of 12)
FULL TANKER
STORAGE & HANDLING UNLOADING
(Step PS2) B C P (Step T7) B C
Yeast,
Processing
Aids FERMENTATION
(Step PS4) C
Processing
Aids, CO2 AGING
(Step PS5) C
CLARIFICATION/ FILTERING
BRIGHT BEER
Bottles, Cans, Kegs, PROCESSING
Crowns, Tankers (Step PS7) C
New
Bottles
Prep
PS8 (NB) PACKAGING
CP (Step PS8)
WAREHOUSING/ SHIPPING
(Step PS9)
RECEIVING
(Step B1) B C P
Storage
(Step B2) B C P
Milling
(Step B3) C
Cereal Cooker
(Step B4)
Mashing
(Step B5)
Lautering
(Step B6)
Holding Tank
(Step B7)
Kettle
(Step B8)
Whirlpool
(Step B9)
Oxygen
Wort Cooling
(Step B10)
COLD WORT
WORT OXYGENATION/
Oxygen/ Sterile WORT AERATION
Air (Step F1 )
Yeast Propagation
(Step Y1)
Yeast Storage
(Step Y2)
Acid Washing
(Step Y3)
FERMENTATION
YEAST
(Step F2)
CO2
Cooling
(Step F3) C
Yeast
Removal
GREEN BEER
(Step F4)
Buffer tank
(Step A2)
Centrifuge
(Step A3)
Yeast,
By-products
Processing aids,
Stabilizers,
CO2, Preservatives Buffer tank
(Step A4)
CO2
Cooling tank
(Step A5) C
CO2, Hops
Aging Tank
(Step A6) C Beer,
Spent Hops, CO2
Deaerated water,
Processing aids,
Stabilizers, CO2,
Preservatives Secondary Storage
(Step A7) C CO2, Spent
Yeast
Deaerated water,
Processing aids,
Stabilizers, CO2,
Preservatives Surge/ Buffer Tank
(Step A8) C
CO2
Caramel & other
ingredients,
Processing aids,
Stabilizers, CO2,
Preservatives Filtration
(Step A9) C
CO2, Spent
Yeast
Deaerated water,
CO2, Nitrogen
Bright Beer Storage
(Step A10 = PS6) C
CO2
CO2
Filtration Flash Pasteurization
(Step SF2) C (Step FP2) C
Process Step 8
PS8 (RB) - RETURNED BOTTLES PREP (Page 7 of 12)
Receiving/ Storage
(Step RB1) P
Caustic
Pre-Rinse
(Step RB6) P
Interior Rinse
(Steps RB12) C P
Water
FINAL RINSE
(Step RB13) C P
Process Step 8
PS8 (NB) - NEW BOTTLES PREP (Page 8 of 12)
Receiving
(Step NB1) P
Preliminary Inspection
(Step NB2) P
Storage
(Step NB3-6) P
Inspection
(Step NB7) P
RINSE
(Steps NB8-9) C P
Process Step 8
PS8 (BT) - BOTTLING (Page 9 of 12)
BOTTLES - See
Returned Bottles Prep
& New Bottle Prep Air
Empty Bottle Inspection
(Steps BT1) C P Drying
Water
(Step BT11)
Storage
(Step BT22)
Live Load
SHIPPING
(Step BT23)
Process Step 8
PS8 (K) - KEGGING (Page 10 of 12)
KEGS
Receiving
(Step K1)
Racking
(Step K7)
Filling (Step K18) C
Storage, Handling,
De-palletizing
(Steps K2-3) Internal Cleaning Internal Cleaning
Manual Automated Barnes Neck Wash &
(Steps K8-12) C (Steps K8-12) C Sanitize
(Step K19-21)
External Inspection
(Step K4 )
Storage
(Step K27)
Live Load
SHIPPING
(Step K28)
Process Step 8
PS8 (C) - CANNING (Page 11 of 12)
CANS
Receiving Drying (Steps C16-17)
(Step C1)
Coding
(Step C6)
Storage & Handling
Fill Height Inspection
(Step C2) B C
(Step C18)
Rinser
Depalletizing/ Pallet ID (Step C7) C
(Steps C3-4 )
Divert to Packers
(Steps C19)
Bright
Beer, Filling
Inspection CO2 (Steps C8- 10)
(Step C5)
CO2
Hi Cone Machine
(Step C20)
Can Ends
Seaming
(Steps C11-13) C
Case Packers
Water (Steps C21)
External Flush
(Step C14)
Pastuerizer Inspection
(Step C15) (Step C22)
Palletize
(Step C25)
Storage
(Step C26)
Live Load
SHIPPING
(Step C27)
Process Step 8
PS8 (T) - TANKERING (Page 12 of 12)
Empty Tanker
(Step T1) C
Caustic, Water,
Acid
Tanker Washing
(Step T2) C
CO2
Tanker Purge
(Step T3) C
CO2
Bright Beer,
CO2
Tanker Filling
(Step T4) B C
Tanker Shipping
(Step T5)
SCHEMATIC DIAGRAM
Note: Each brewery must be individually assessed at the time of implementation to ensure identified
hazards have been addressed.
Schematic Diagram
TO BE COMPLETED
HAZARD IDENTIFICATION
BIOLOGICAL HAZARDS
INGREDIENTS
LIQUID INGREDIENTS
DRY INGREDIENTS
OTHER INGREDIENTS
PROCESS STEPS
PS3 - BREWING
PS4 -FERMENTATION
PS8 RB
RETURNED BOTTLES PREP
(FLOAT GLASSWARE PREP)
PS8 NB -
NEW BOTTLES (GLASSWARE)
PREP
PS8 BT - BOTTLING
K7 None identified
Racking
PS8 T -
TANKERING
HAZARD IDENTIFICATION
CHEMICAL HAZARDS
List all chemical hazards related Identified chemical hazards Controlled at:
to ingredients, incoming
material, processing, product
flow, etc.
INGREDIENTS
LIQUID INGREDIENTS
DRY INGREDIENTS
OTHER INGREDIENTS
PROCESS STEPS
PS1- RECEIVING Chemical Contamination
from truck (damage, leaks,
odors)
PS3 - BREWING
PS4 -FERMENTATION
PS8 RB
RETURNED BOTTLES PREP
(FLOAT GLASSWARE PREP)
PS8 NB -
NEW BOTTLES (GLASSWARE)
PREP
PS8 BT - BOTTLING
BT1 MACHINE:
Empty Bottle Inspection Failure of the system to detect
(Human or Machine residual liquid and caustic
inspection)
HUMAN:
Failure of personnel to detect
residual liquid
K7 None identified
Racking
Manual
Cleaning solution not
effectively removed.
PS8 T -
TANKERING
INGREDIENTS
LIQUID INGREDIENTS
DRY INGREDIENTS
OTHER INGREDIENTS
Salt Rocks
PROCESS STEPS
PS3 - BREWING
PS4 -FERMENTATION
F3 - Cooling
PS4 SUB-PROCESS
YEAST PREPARATION
PS5 - AGING/
CLARIFICATION/
FILTRATION
A1 - Cooling
PS7(FP) Flash
Pasteurization
PS8 RB
RETURNED BOTTLES PREP
(FLOAT GLASSWARE PREP)
Bottle plugged
PS8 NB -
NEW BOTTLES
(GLASSWARE) PREP
PS8 BT - BOTTLING
BT1 MACHINE:
Empty Bottle Inspection Failure of the system to detect
(Human or Machine foreign matter, glass defects,
inspection) bottle damage
HUMAN:
Failure of personnel to detect
foreign matter, glass defects,
glass damage
Auto-Flush
Burst bottle leading to glass
inclusion
Manual Flush
Burst bottle leading to glass
inclusion
MACHINE:
Physical Failure to detect
foreign matter (including glass)
K7 None identified
Racking
PS8 T -
TANKERING
CRITICAL CONTROL
POINTS
Incoming Category Determine if fully controlled by Q1. Could a Q2. Is it Q3. Is this Q4. Will a CCP
material/ process and Pre-requisite program. control likely that process subsequen Number
step/ hazards on identified measure(s) contaminati step t step
schematic hazard. *If yes = indicate Pre-requisite be used by on with the specificall eliminate + proceed
diagram Program and proceed to next the operator identified y the to next
identified hazard. at any hazard designed identified identified
process could to hazard or hazard
*If no = proceed to question1 (Q1). step? occur in eliminate/ reduce
excess of reduce likely
If NO = not a the the likely occurrenc
CCP + acceptable occurrenc e to an
identification level or e of the acceptable
on how this could identified level?
hazard will be increase to hazard to
controlled an an If NO = CCP + go to last
before and unacceptab acceptabl column
after the le level? e level?
process If YES =
If NO = not If NO = not a CCP
+ proceed to a CCP + next + identify
the next proceed to question subsequent
identified the next (Q4) step +
hazard identified proceed to
hazard If YES = the next
If YES = CCP + go identified
description + If YES = to last hazard
next question next column
(Q2) question
(Q3)
INGREDIENTS
LIQUID INGREDIENTS
WATER
DRY INGREDIENTS
Physical
Glass, Metal
+ COA, Inspection
OTHER INGREDIENTS
Yeast Biological
Cross
contaminated
e.g.
Salmonella
Carbohydrate Biological
Matt Clostridium
er
Chemical PP Transportation, Receiving &
(e.g. sucrose, Antibiotic Storage (BAC B1.1)
syru residue,
p, heavy metal + COA
hone (honey)
y)
Physical PP Transportation, Receiving &
None Storage (BAC B1.1)
identified
+ COA
(Partially Controlled)
+ Inspection
+ COA, Inspection
+ COA, Inspection
Nitrogen/ Biological
Oxygen/ None
Compressed Air Identified
Physical
None
identified
Caramel Biological
None
identified
Dextrin Biological
None
identified
Stabilizing Biological
Agents None
identified
Physical
None
identified
Water Biological
preparation None
agents identified
Physical
None
identified
Preservatives Biological
None
identified
Physical
None
identified
Chemical
None
identified
+COA, Inspection
Yes
RLD
Physical - No Yes Bottle
Critical Glass Wash No Yes
Defects , Dirt, Empty
Dust, Glass, Bottle
Syringes, Inspection
Medical
Patches,
Chemical
None
identified
+COA
Chemical
None
identified
Chemical
None
identified
Physical
None
identified
Chemical
None
identified
Physical
None
identified
Crowns Biological
None
identified
Chemical
None
identified
Physical
None
identified
Chemical
None
identified
Physical
None
identified
PROCESS STEPS
Physical
Pests in hoses PP Transportation, Receiving &
used for Storage (BAC B1.1)
transferring
material, Bulk + Seal Integrity
Receiving
PP - Pest Control (BAC E2.1)
+ Training
PS3 - BREWING
PS4
-FERMENTATION
PS4 SUB-
PROCESS
YEAST
PREPARATION
PS5 - AGING/
CLARIFICATION/
FILTRATION
Cleaning
chemicals
PS7 BRIGHT
BEER
PROCESSING
PS7 (SF)
Sterile Filtration
PS7(FP) Flash
Pasteurization
PS8 RB
RETURNED
BOTTLES PREP
(FLOAT
GLASSWARE
PREP)
Training
Training
Training
Training
Chemical - Training
Bottle unable to
drain No Yes (EBI/ Yes No Yes(EBI/
RLD) RLD)
Physical -
Damage to Yes (EBI)
bottles,
Physical
Bottle contains Yes (EBI)
foreign object PP Equipment (BAC C1.2)
(plugged but
sprays cannot
clear object) Yes (EBI/
No RLD) Yes No Yes (EBI)
Chemical
Bottle unable to
drain
RB9- Post-Soak Physical - (Partially Controlled) Yes (EBI) Yes No Yes (EBI)
Damage to
bottles (e.g. PP Equipment (BAC C1.2)
Temperature
shock), PP Personnel (BAC D1.2)
Training
Physical - Yes (EBI) Yes No Yes (EBI)
Bottle plugged
Chemical No
Bottle unable to Yes (EBI/ Yes No Yes (EBI/
drain RLD) RLD)
No
RB10 - External Physical - (Partially Controlled) Yes (EBI) Yes No Yes (EBI)
Flush Damage to
bottles (e.g. PP Equipment (BAC C1.2)
Temperature
shock) PP Personnel (BAC D1.2)
Training
RB11 - Ext. Rinse Physical - (Partially Controlled) Yes (EBI) Yes No Yes (EBI)
Damage to
bottles PP Equipment (BAC C1.2)
(e.g.
Temperature PP Personnel (BAC D1.2)
shock) Training
RB12 - Interior Physical - (Partially Controlled) Yes (EBI) Yes No Yes (EBI)
Rinse Damage to
bottles PP Equipment (BAC C1.2)
Physical -
Bottle contains
foreign object
(spray
malfunction)
Chemical
Spray No Yes (EBI) Yes No Yes (EBI)
malfunction
PP Equipment (BAC C1.2) Yes (EBI/ Yes No Yes (EBI/
Chemical - RLD) RLD)
Bottle plugged
unable to drain
No
RB13 - Final Physical - (Partially Controlled) Yes (EBI) Yes No Yes (EBI)
Rinse Damage to
bottles, PP Equipment (BAC C1.2)
Physical -
Bottle contains
foreign object PP Equipment (BAC C1.2)
(spray
malfunction)
Physical
Bottle contains
foreign object
(plugged but
sprays cannot No Yes (EBI) Yes No Yes (EBI)
clear object)
Chemical
Bottle unable to
drain
No Yes (EBI/ Yes No Yes (EBI/
RLD) RLD)
PS8 NB -
NEW BOTTLES
(GLASSWARE)
PREP
NB7 Inspection Physical (Partially Controlled) Yes (EBI) Yes No Yes (EBI)
(Human, visual) Missed critical
glass defects PP Personnel (BAC D1.2)
Training
Training
PS8 BT -
BOTTLING
Empty Bottle Physical - (Partially Controlled) Yes (EBI) Yes Yes CCP1-P
Inspection Failure of the
system to PP Equipment (BAC C1.2)
Human or detect foreign
Machine matter, glass PP Personnel (BAC D1.2)
inspection (EBI/ defects, bottle Training
RLD) damage
Chemical -
Failure of the
system to
detect residual
liquid and
caustic
Yes (EBI/ Yes Yes CCP1-C
HUMAN: (Partially Controlled) RLD)
Physical -
Failure of PP Equipment (BAC C1.2)
personnel to
detect foreign PP Personnel (BAC D1.2)
matter, glass Training
defects, glass
damage HUMAN:
(Partially Controlled) Yes (EBI) Yes Yes CCP1-P
Chemical -
Failure of PP Personnel (BAC D1.2)
personnel to Training, SOP (personnel rotation)
detect residual
liquid (Partially Controlled)
Yes (EBI Yes Yes CCP1-C
PP Personnel (BAC D1.2)
Training
equipment),
glass inclusion
(Partially Controlled)
Manual Flush:
Chemical
Lubricants
PS8 (K) -
KEGGING
K7 None identified
Racking
Chemical
Cleaning
solution not No Yes Yes Yes CCP3-C
effectively Manual:
removed.
(Partially Controlled)
K 16 - K17
Barnes Neck
Sanitize & Inspect
PS8 (C) -
CANNING
PS8 T -
TANKERING
COA
FORM 3A:
Page 1 of 12
KEY
MASTER FLOWCHART OF
MAJOR PROCESS STEPS (PS) FOR MAKING BEER (Page 2 of 12)
FULL TANKER
STORAGE & HANDLING UNLOADING
(Step PS2) (Step T7)
Yeast,
Processing
Aids FERMENTATION
(Step PS4)
Processing
Aids, CO2 AGING
(Step PS5)
CLARIFICATION/ FILTERING
BRIGHT BEER
Bottles, Cans, Kegs, PROCESSING
Crowns, Tankers (Step PS7)
New
Bottles
Prep PACKAGING
PS8 (NB) (Step PS8)
BOTTLING KEGGING
Returned CANNING TANKERING
Step PS8 (BT) Step PS8 (K)
Bottles Step PS8 (C) Step PS8 (T)
CCP1-C,P CCP3-C
Prep
PS8 (RB) CCP2-P
- Washing
- Rinsing - Cleaning
- Inspection
- Filling - Filling - Filling
- Filling
- Packing - Palletizing
- Flushing
WAREHOUSING/ SHIPPING
(Step PS9)
RECEIVING
(Step B1)
Storage
(Step B2)
Milling
(Step B3)
Cereal Cooker
(Step B4)
Mashing
(Step B5)
Lautering
(Step B6)
Holding Tank
(Step B7)
Kettle
(Step B8)
Whirlpool
(Step B9)
Oxygen
Wort Cooling
(Step B10)
COLD WORT
WORT OXYGENATION/
Oxygen/ Sterile WORT AERATION
Air (Step F1 )
Yeast Propagation
(Step Y1)
Yeast Storage
(Step Y2)
Acid Washing
(Step Y3)
FERMENTATION
YEAST
(Step F2)
CO2
Cooling
(Step F3)
Yeast
Removal
GREEN BEER
(Step F4)
Buffer tank
(Step A2)
Centrifuge
(Step A3)
Yeast,
By-products
Processing aids,
Stabilizers,
CO2, Preservatives Buffer tank
(Step A4)
CO2
Cooling tank
(Step A5)
CO2, Hops
Aging Tank
(Step A6) Beer,
Spent Hops, CO2
Deaerated water,
Processing aids,
Stabilizers, CO2,
Preservatives Secondary Storage
(Step A7) CO2, Spent
Yeast
Deaerated water,
Processing aids,
Stabilizers, CO2,
Preservatives Surge/ Buffer Tank
(Step A8)
CO2
Caramel & other
ingredients,
Processing aids,
Stabilizers, CO2,
Preservatives Filtration
(Step A9)
CO2, Spent
Yeast
Deaerated water,
CO2, Nitrogen
Bright Beer Storage
(Step A10 = PS6)
CO2
CO2
Filtration Flash Pasteurization
(Step SF2) (Step FP2)
Process Step 8
PS8 (RB) - RETURNED BOTTLES PREP (Page 7 of 12)
Receiving/ Storage
(Step RB1)
Caustic
Pre-Rinse
(Step RB6)
Interior Rinse
(Steps RB12)
Water
FINAL RINSE
(Step RB13)
Process Step 8
PS8 (NB) - NEW BOTTLES PREP (Page 8 of 12)
Receiving
(Step NB1)
Preliminary Inspection
(Step NB2)
Storage
(Step NB3-6)
Inspection
(Step NB7)
RINSE
(Steps NB8-9)
Process Step 8
PS8 (BT) - BOTTLING (Page 9 of 12)
BOTTLES - See
Returned Bottles Prep
& New Bottle Prep Air
Empty Bottle Inspection
(Steps BT1) Drying
Water
CCP1-C, P (Step BT11)
Storage
(Step BT22)
Live Load
SHIPPING
(Step BT23)
Process Step 8
PS8 (K) - KEGGING (Page 10 of 12)
KEGS
Receiving
(Step K1)
Racking
(Step K7)
Filling (Step K18)
Storage, Handling,
De-palletizing Internal Cleaning
(Steps K2-3) Manual Internal Cleaning
(Steps K8-12) Automated Barnes Neck Wash &
(Steps K8-12) Sanitize
CCP3-C
(Step K19-21)
External Inspection
(Step K4 )
Storage
(Step K27)
Live Load
SHIPPING
(Step K28)
Process Step 8
PS8 (C) - CANNING (Page 11 of 12)
CANS
Receiving Drying (Steps C16-17)
(Step C1)
Coding
(Step C6)
Storage & Handling
Fill Height Inspection
(Step C2)
(Step C18)
Rinser
Depalletizing/ Pallet ID (Step C7)
(Steps C3-4 )
Divert to Packers
(Steps C19)
Bright
Beer, Filling
Inspection CO2 (Steps C8- 10)
(Step C5)
CO2
Hi Cone Machine
(Step C20)
Can Ends
Seaming
(Steps C11-13)
Case Packers
Water (Steps C21)
External Flush
(Step C14)
Pastuerizer Inspection
(Step C15) (Step C22)
Palletize
(Step C25)
Storage
(Step C26)
Live Load
SHIPPING
(Step C27)
Process Step 8
PS8 (T) - TANKERING (Page 12 of 12)
Empty Tanker
(Step T1)
Caustic, Water,
Acid
Tanker Washing
(Step T2)
CO2
Tanker Purge
(Step T3)
CO2
Bright Beer,
CO2
Tanker Filling
(Step T4)
Tanker Shipping
(Step T5)
BIOLOGICAL HAZARDS
CONTROL & CCPS
INGREDIENTS
LIQUID INGREDIENTS
DRY INGREDIENTS
+ COA
OTHER INGREDIENTS
+ COA
+ COA
+COA
+ COA
PROCESS STEPS
PS3 - BREWING
PS4 -FERMENTATION
PS8 RB
RETURNED BOTTLES PREP
(FLOAT GLASSWARE PREP)
PS8 NB -
NEW BOTTLES (GLASSWARE)
PREP
PS8 BT - BOTTLING
K7 None identified
Racking
PS8 T -
TANKERING
T6 T7 Full Tanker Receiving & Insect or pest infestation No pathogens known to survive
Unloading of hoses in final product due to
properties of beer, e.g. low pH,
alcohol content see Form 1
CHEMICAL HAZARDS
CONTROL & CCPS
Title: Form 6A
BAC Generic Hazard Identification - Chemical Hazards Control & CCPs
Completed By: BAC TC Date:
Approved By: BAC TC Date:
INGREDIENTS
LIQUID INGREDIENTS
DRY INGREDIENTS
+ COA
+ COA
COA
+ COA
+ COA
+ COA
+ COA
+ COA
+ COA,
+ COA
+ Inspection,
PROCESS STEPS
PS3 - BREWING
PS4 -FERMENTATION
PROCESS STEPS
PS4 SUB-PROCESS
YEAST PREPARATION
PS5 - AGING/
CLARIFICATION/
FILTRATION
PS7(FP) Flash
Pasteurization
PS8 RB
RETURNED BOTTLES
PREP (FLOAT
GLASSWARE PREP)
RB7 - Soak Tanks With Too concentrated, too low, PP Equipment (BAC C1.2)
Caustic no caustic, wrong chemical
PP Transportation, Receiving &
Bottle unable to drain Storage (BAC B1.1)
RB8 - Hydro Jet Sprays Bottle unable to drain EBI (Empty Bottle
Inspection)/RLD(Residual Liquid
Detector)
PS8 NB -
NEW BOTTLES
(GLASSWARE) PREP
NB9 - Bulk Glass Rinser Contaminated air, sanitizing PP Equipment (BAC C1.2)
spray
PP Personnel (BAC D1.2) Training
PS8 BT - BOTTLING
CCP1-C
PROCESS STEPS (Continued)
BT12 BT13 Labelling, Product not coded or not PP - Recall (BAC F1.2)
Coding correctly coded
PP Equipment (BAC C1.2)
BT19 BT20 Secondary Product not coded or not PP - Recall (BAC F1.2)
Code & Inspection correctly coded
(Secondary Packaging, PP Equipment (BAC C1.2)
Code/Inspection)
K7 None identified
Racking
Manual Manual
CCP3-C
C2 - Storage & Handling Contamination from leaking PP Premises (BAC A1.1 & BAC A2.1)
roof or pipes
C7 - Bulk in-line rinser Chemicals from PP Premises (BAC A1.1 & BAC A2.1)
compressed air or water
PP Equipment (BAC C1.2)
C23 C24 Tray Machine Incorrect or missing code PP - Recall (BAC F1.2)
& Code
PP Equipment (BAC C1.2)
PS8 T -
TANKERING
COA
PHYSICAL HAZARDS
CONTROLS & CCPS
Title: Form 7A
BAC Generic Hazard Identification - Physical Hazards Control & CCPs
Completed By: BAC TC Date:
Approved By: BAC TC Date:
INGREDIENTS
LIQUID INGREDIENTS
DRY INGREDIENTS
+ COA, Inspection
OTHER INGREDIENTS
+ Inspection
+ COA, Inspection
+ COA, Inspection
+ COA
+ COA
+ COA
+COA, Inspection
+COA
+ Rinse
Rinse
PROCESS STEPS
PS3 - BREWING
PS4 -FERMENTATION
F3 - Cooling
PS4 SUB-PROCESS
YEAST PREPARATION
PS5 - AGING/
CLARIFICATION/
FILTRATION
A1 - Cooling
PS7(FP) Flash
Pasteurization
PS8 RB
RETURNED BOTTLES
PREP (FLOAT
GLASSWARE PREP)
+EBI
+EBI
+EBI
PS8 NB -
NEW BOTTLES
(GLASSWARE) PREP
+EBI
NB9 - Bulk Glass Rinser Spray malfunction (e.g. PP Equipment (BAC C1.2)
plugged sprays)
PS8 BT - BOTTLING
CCP1-P
HUMAN: HUMAN:
Failure of personnel to detect (Partially Controlled)
foreign matter, glass defects, PP Personnel (BAC D1.2) Training,
glass damage SOP (personnel rotation)
CCP1-P
BT2 Down Bottle Filler Glass inclusions from PP Equipment (BAC C1.2)
In-Feed Control breakage of down bottle at
filler in-feed PP Personnel (BAC D1.2)
BT3 BT5 Filling Chipping of bottles (e.g. from PP Equipment (BAC C1.2)
(Purges , Filling, Fobbing) filling equipment), glass
inclusion PP Personnel (BAC D1.2) Training
Auto-Flush Auto-Flush
CCP2-P
Manual Flush Manual Flush
BT12 BT13 Labelling, Product not coded or not PP - Recall (BAC F1.2)
Coding correctly coded
PP Equipment (BAC C1.2)
BT19 BT20 Secondary Product not coded, or not PP - Recall (BAC F1.2)
Code & Inspection correctly coded
(Secondary Packaging, PP Equipment (BAC C1.2)
Code/Inspection)
K7 None identified
Racking
C23 C24 Tray Machine Incorrect or missing code PP - Recall (BAC F1.2)
& Code
PP Equipment (BAC C1.2)
PS8 T -
TANKERING
Hazards (B = Biological, C=Chemical, P= Physical) Indicate the way the Hazard could be
Addressed (Cooking Instructions,
Public Education, Use Before Date,
etc.)
Hazard Descriptions
HACCP PLAN
CCP/
Process Hazard Hazard Critical Monitoring Deviation Verification HACCP
Steps Number Description Limits procedures Procedures Procedures Records
Empty Bottle CCP1-P Physical - EBI test Who Packaging If the CCP test fails, Pre-start EBI Test Bottle
Inspection- EBI Failure of the bottle failure Operator/ QA the line is stopped by check Monitoring
(Step BT1) system to personnel Packaging Operator/ completed on Records
detect foreign (i.e. 100% QA. Manager/ system by
matter, glass test bottle Frequency At start Supervisor is electricians. Corrective
defects, bottle rejection) up, hourly and at end notified. Action Records
damage of shift Line
Hold product from Supervisor Verification
Refer to SOP last successful test reviews Records
describing EBI testing. records after
100% inspection of each shift or Product Hold &
The Packaging product since last daily and Inspection
Operator or QA successful test is signs & dates Records
personnel signs and done (accept/ reject records.
dates the EBI Test product). Product
Bottle Monitoring Monthly QA Destruction
Form. Repair/ fix equipment record Records
and verify. review.
CCP/
Process Hazard Hazard Critical Monitoring Deviation Verification HACCP
Steps Number Description Limits procedures Procedures Procedures Records
Empty Bottle CCP1-C Chemical - RLD test Who Packaging If the CCP test fails, Pre-start RLD Test Bottle
Inspection Failure of the bottle failure Operator/ QA the line is stopped by check Monitoring
/Residual Liquid system to personnel Packaging Operator/ completed on Records
Detector detect residual (i.e. 100% QA. Manager/ system by
liquid and test bottle Frequency At start- Supervisor is notified. electricians. Corrective
EBI/RLD caustic rejection) up, hourly and at end Action Records
of shift Hold product from Line
(Step BT1) last successful test Supervisor Verification
Refer to SOP reviews Records
describing RLD Product is discarded. records after
testing. each shift or Product
daily and Destruction
The Packaging signs & dates Records
Operator or QA records.
personnel signs and
dates the RLD Test Monthly QA
Bottle Monitoring record
Form. review.
CCP/
Process Hazard Hazard Critical Monitoring Deviation Verification HACCP
Steps Number Description Limits procedures Procedures Procedures Records
- Re-inspect 100% of
product since last
successful check
(accept / reject
product).
CCP/
Process Hazard Hazard Critical Monitoring Deviation Verification HACCP
Steps Number Description Limits procedures Procedures Procedures Records
Internal CCP3-C Chemical Rinse water Who - Kegging If the CCP fails: QA personnel Keg Cleaning
Cleaning Cleaning visible in Operator will perform a Records
(Manual) solution not sight glass of The Kegging Operator sodium check
effectively test keg. Frequency Start up, notifies the Line on the test Analytical
(Steps K8 K12) removed. *every 24 kegs and at Supervisor and keg from the Results
describes the failure.
No the completion of start of each
detectable kegging operation production Corrective
If the rinse water is not
caustic carry- visible through the sight
run. Action Report
over based Perform a visual check glass and/or the
on for rinse water and phenolphthalein check Sodium in the Verification
phenolphthal phenolphthalein check is positive for caustic test keg Reports
ein check. for caustic carry over (turns pink), the sample must
Kegging Operator meet the CCP Monthly
Refer to SOP for performs 2 additional Canadian Audit
test keg runs and if Drinking
details.
either of the re-test fails
Water CCP Training
a CCP failure has
Note: Frequency of occurred. If both re-test Guidelines of Records
every 24 Kegs is for passes, production may <200mg/L of
example purposes resume. sodium.
only. Frequency
should be determined Production may resume The
based off current when the problem has Supervisor
operations (i.e. rate been corrected and verifies the
and number of bottles confirmed by 2 keg rinse
consecutive test keg reports daily.
produce)
runs.
CCP/
Process Hazard Hazard Critical Monitoring Deviation Verification HACCP
Steps Number Description Limits procedures Procedures Procedures Records
Deviations and
Corrective Actions are
recorded on the
Corrective Action
Report by the
Supervisor.
FORM 3
PS9 Warehousing/Shipping
Ps3 - Brewing
Sparge water, Steam B6 Lautering (Lauter Tun, Mash Spent Grains, Sweet
Filter removal of spent grains Water
B7 Holding Tank
Ps4 - Fermentation
Ps5 - Aging/Clarification/Filtration
A2 Buffer Tank
Preservatives
A5 Cooling
Preservatives
Preservatives
Caramel and other A9 DE Pre-filter/ Filter Trap/ Sheet Spent DE, Spent
ingredients, Filter/ Membrane Filter/ PVPP Yeast, Spent Hops,
Processing Aids, Filter CO2,
Stabilizers, CO2,
Nitrogen
Preservatives
A Sterile Filtration
B Flash Pasteurization
FP2 Pasteurized
Beer Tank
Steam, water, chemicals RB7 Soak Tanks With Label pulp, Caustic
Caustic (Sodium Hydroxide),
Plastic
Washed Glassware
NB3 Storage
Bottling
Compressed Air,
Conveyor Lubricant,
CO2, Compressed Air, BT3 Purges & Evacuation & Glass, debris,
Positive Pressure shards
Potable Water, Lube
Water CO2
City Water Flush BT7 Crowner Flush (external) Water and beer
effluent
Bottling (Continued)
BT23 Shipping
Kegging
Kegging (Continued)
K28 Shipping
Canning
CO2 & Bright beer C8 Filling (pre-evacuation & Open filled cans
beer fill)
Rinse water (Bulk Rinse C14 External Can Flush Water to sewer
discharge water)
1
Output from one step may be used as input to another step (indicated by bolded print)
Canning (Continued)
C27 Shipping
Ps8 (T)
Tankering
T1 Empty Tanker
T5 Tanker Shipping
(No Flowchart)
CO5 Compressor
CO10 Vaporization
(No Flowchart)
CO2
FORM 8
CRITICAL COTNROL
POINTS
(LOW ALCOHOL BEER)
Incoming Category Determine if fully controlled by Q1. Could a Q2. Is it Q3. Is this Q4. Will a CCP
material/ process and Pre-requisite program. control likely that process subsequen Number
step/ hazards on identified measure(s) contaminati step t step
schematic hazard. *If yes = indicate Pre-requisite be used by on with the specificall eliminate + proceed
diagram Program and proceed to next the operator identified y the to next
identified hazard. at any hazard designed identified identified
process could to hazard or hazard
*If no = proceed to question1 (Q1). step? occur in eliminate/ reduce
excess of reduce likely
If NO = not a the the likely occurrenc
CCP + acceptable occurrenc e to an
identification level or e of the acceptable
on how this could identified level?
hazard will be increase to hazard to
controlled an an If NO = CCP + go to last
before and unacceptab acceptabl column
after the le level? e level?
process If YES =
If NO = not If NO = not a CCP
+ proceed to a CCP + next + identify
the next proceed to question subsequent
identified the next (Q4) step +
hazard identified proceed to
hazard If YES = the next
If YES = CCP + go identified
description + If YES = to last hazard
next question next column
(Q2) question
(Q3)
PS3 - AGING/
CLARIFICATION/
FILTRATION
Chemical
None
identified
Physical
None
identified
FORM 10
ADDITIONS FOR
LOW ALCOHOL BEER
PRODUCT NAME:
Bright Beer CCP4-B Inadequate pH pH <4.5 pH analysis of pH must be less pH analysis performed on each kettle Lab
Storage (Step adjustment to wort in kettle by than 4.4 at kettle wort cooler sample & result reviewed reports
(Note: This
A10) control QA wort sample in by QA manager or designate (if
is an Calibratio
Clostridia kettle greater than pH 4.5 will reprocess and
arbitrary n records
growth recheck)
number. - If pH greater than
downstream Audit
CCP or equal to 4.4 pH analysis performed on each BBT &
records
numbering will add additional result reviewed by QA manager or
will depend acid to kettle & designate (if greater than pH 4.5 will
on the recheck. reprocess and recheck)
number of
- If pH greater than pH analysis performed on each filler
CCPs
or equal to 4.4 start up sample & result reviewed by
found in
QA manager (or QA manager or designate (if greater
individual
designate) than pH 4.5 will dump product)
breweries
notified and a
CCPs) Calibration of pH meter & control
deviation report
checks of 5 samples prior to run.
must be
completed After each production the QA Manager
or designate verifies the calibration
records for BBT approvals.
QA Manager conducts yearly audit of
lab analyses.
DIAGRAMS FOR
HAZARD IDENTIFICATION &
CCP DECISION TREE
Critical Control Points for breweries were determined using the HACCP Decision
Tree. The Decision Tree was first developed by a Codex Alimentarius working
group on HACCP in June 1991.
These questions are to be answered for each potential hazard at each step:
YES NO NO YES
No Hazard*
NO NO
YES
No Hazard*
YES
No C.M. exists
C.M.(S) exists
Not a CCP. Identify how this hazard will
be controlled before or after the process
and proceed to next identified hazard.
Q2 Is it likely that contamination with the identified hazard could occur in excess of
the acceptable level or could increase to an unacceptable level?
No
Yes
No Yes = CCP
Q4 Will a subsequent step eliminate the identified hazard or reduce its likely
occurance to an acceptable level?
Yes No = CCP
In 1988, a BAC Glass Integrity Task Force developed a manual entitled Good
Manufacturing Practice on the Prevention of Glass Inclusion in Finished Product.
As its name implies, it was intended to ensure that product entering the market
contained no glass contaminants. The GMP was updated 1998 to deal with
changes in the industry and technology in the last 10 years.
Environmental Controls
Preventive Measures
Regular Maintenance Checks
Bottle Washing
Preventive Measures
Foam-Picking
Candling
Filtration
Reaction to Inclusions
Written Procedures
Production Records
Quality Checklists
BLANK FORMS 1 - 10
1. Product Name(s)
3. How it is to be Used
4. Packaging
5. Shelf Life
7. Labelling Instructions
PRODUCT NAME:
PRODUCT NAME(S):
PRODUCT NAME(S):
PRODUCT NAME(S)
List all biological hazards related to ingredients, incoming material, processing, product
flow, etc.
PRODUCT NAME(S)
List all chemical hazards related to ingredients, incoming material, processing, product
flow, etc.
PRODUCT NAME(S)
List all physical hazards related to ingredients, incoming material, processing, product
flow, etc.
Process Step/ Category and Q1. Could a control Q2. Is it likely that Q3. Is this process Q4. Will a CCP Number
Incoming Material identified Hazard measure(s) be contamination with step specifically subsequent step
used at any the identified designed to eliminate the
process step? hazard could occur eliminate/reduce hazard or reduce
in excess of the the likely its likely
Fully controlled by acceptable level or occurrence of the occurrence to an
Pre-requisite could increase to identified hazard to acceptable level?
program? *If no = not CCP. an unacceptable an acceptable
Identify how this level? level?
hazard will be
controlled before *If no = CCP. Go to
*If yes indicate and and after the last column
proceed to next process and proceed *If no = not CCP. *If no = proceed to
identified hazard to next identified Proceed to next (Q4)
hazard. identified hazard
*If yes = not a CCP.
Identify subsequent *Proceed to the next
*If no proceed to *If yes = CCP. Go to step and proceed to identified hazard
(Q1) *If yes = describe *If yes = proceed to last column the next identified
and proceed to (Q2) (Q3) hazard
REFERENCE LITERATURE
A Simple Guide to Understanding and Applying The Hazard Analysis Critical Control
Point Concept. 2nd edition. international Life Sciences Institute. 1997